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Pituitary gland Saddam Ansari Tbilisi State Medical University
Disorders of Pituitary Gland
Causes of Disorder of Pituitary Gland  Mainly of 2 reasons: Hyperactivity Hypoactivity
Disorders of Pituitary Gland
Disorders of Pituitary Gland
Gigantism Pituitary disorder characterized by: Excess growth of body Average height is approximately 7 – 8 feet
Continued… Causes of Gigantism Hypersecretion of GH in childhood or in pre – adult  Tumor of acidophilic cells of  Anterior pituitary
Continued… Signs and Symptoms Huge stature : 7 or 8 feet height Hyperglycemia , develop glycosuria , pituitary diabetes mellitus Headache due to tumor of pituitary
Continued… Visual disturbances  Gigantism ends in hypopituitarism (burning of cells of anterior pituitary )
Disorders of Pituitary Gland
Acromegaly  Anterior pituitary disorder characterized by: Enlargement, thickening, and broadening of bones Particularly extremities of the  body
Continued… Causes of Acromegaly Hypersecretion of GH after fusion of epiphysis with shaft of bone Adenomatous tumor of anterior pituitary involving the acidophilic cells.
Continued... Signs and symptoms ,[object Object],Supraorbital ridges Broadening of nose  Thickening of lips Thickening and wrinkles formation on forehead Lower jaw (prognathism) Face with these features called as acromegalic or guerilla face
Continued… Signs and symptoms Kyphosis : enlargement of hands and feet with bowing spine  Scalp is thickened and thrown into folds Overgrowth of body hair Visceral organs are enlarged
Continued… Signs and symptoms Thyroid , parathyroid and adrenal glands shows hyperactivity Hyperglycemia and glucosuria Hypertension Headache Visual disturbance – Bitemporal hemianopia
Disorders of Pituitary Gland
Acromegalic Gigantism ,[object Object]
Due to hypersecretion of GH in children,before fusion of epiphysis with the shaft of bone results in Gigantism
If hyersecretion of GH is continued after the fusion of          epiphysis the symptoms of Acromegaly also appear,[object Object]
Disorders of Pituitary Gland
Cushing’s Disease Rare disease characterized by obesity
Continued… Cause Hypersecretion of glucocorticoids mainly cortisol Either pituitary origin or adrenal origin              Cushing’s               Cushing’s             disease                   syndrome
Continued… Pituitary origin Increased secretion of ACTH leads to hyperplasia of adrenal cortex therefore, hypersecretion of glucocorticoids takes place ACTH is increased by Tumor in pituitary cells ( basophilic cells) Malignant tumor of nonendocrine origin like cancer of lungs or abdominal viscera Hypothalamic disorder causing hypersecretion of corticotropin releasing hormone
Continued… Signs and symptoms 1. Disproportionate distribution of body fat results: Moon face : Fat accumulation and retention of water and salt  Torso : Fat accumulation in chest and abdomen but slim legs and arms Buffalo hump : Fat deposit on the back of neck and shoulder Pot belly : Fat accumulation in upper abdomen
Continued… 2. Purple striae : Reddish purple stripes on abdomen due to mainly three reasons: ,[object Object]
Rupture of subdermal tissues due to stretching
Deficiency of collagen fibres due to protein depletion,[object Object]
Continued… 3. Thinning of extremities 4. Thinning of skin and subcutaneous tissues 5. Darkening of skin on neck (aconthosis) 6. Pigmentation of skin  7. Facial redness (facial plethora) 8. Weakening of muscle
Continued… 9. Facial hair growth ( Hirsutism ) 10. Bone resorption leads to osteoporosis 11. Hyperglycemia due to gluconeogeneis leads adrenal diabetes and glycosuria 12. Hypertension 13. Immunosuppression resulting in susceptibility for infection 14. Poor  healing
Disorders of Pituitary Gland
Dwarfism Pituitary disorder in children characterized by stunted growth
Cause of Dwarfism Reduction in the GH in infancy or early childhood Occurs because of following reasons: ,[object Object]
Deficiency of Somatomedin – C
Atrophy of acidophilic cells in the adenohypophysis
Tumor of  chromophobes : nonfunctioning tumor , compresses and destroys the normal cells
Panhypopituitarism,[object Object]
Types of Dwarfism Laron dwarfism Psychogenic dwarfism Dwarfism in dystrophiaadiposogenitalis
Laron Dwarfism Genetical disorder Called as GH insensitivity Occurs due to presence of abnormal GH secretagogue receptors in liver GHS becomes abnormal due to mutation in genes responsible for receptor Doesn’t depend on amount of GH secretion , hormone can’t stimulate the growth due to abnormal GHS
Psychogenic Dwarfism Due to extreme emotional deprivation or stress Deficiency of GH Also called as psychosocial dwarfism or Stress dwarfism
Dwarfism in Dystrophiaadiposogenitalis Called as Frohlich syndrome Rare childhood disorder Characterized by : ,[object Object]
Growth retardation
Retarded development of genital organs
Associated with tumors of hypothalamus – increased appetite and decrease in gonadotropin hormone,[object Object]
Acromicria Rare disease in adults characterized by the atrophy of the extremities of the body
Causes of Acromicria Deficiency of GH in adults Secretion of GH  decreases in the following conditions: ,[object Object]
Atrophy of acidophilic cells in the anterior pituitary
Tumor of chromophobes
Panhypopituitarism,[object Object]
Signs and Symptoms Atrophy and thinning of extremities ( major symptoms ) Associated with hypothyroidism Hyposecretion of adrenocortical hormone Person becomes lethargic and obese Loss of sexual function
Disorders of Pituitary Gland
Simmond’s Disease Rare pituitary disease Also called as cachexia Occurs mostly in panhypopituitarism
Signs and Symptoms Developing senile decay  Senile decay is due to deficiency of hormone from target glands of anterior pituitary e.g. thyroid gland, adrenal cortex and the gonads Loss of hair and loss of teeth The skin on face becomes dry and wrinkled. ( most common )
Summary…..
Disorders of Pituitary Gland
Syndrome of Inappropriate Hypersecretion of Antidiuretic hormone  Disease characterized by loss of sodium through urine due to hypersecretion of ADH
Causes Due to cerebral tumors, lung tumors and lung cancers because the tumor cells  secrete ADH Normal secretion of  ADH makes the plasma hypotonic Hypotonic solution inhibits the ADH secretion and restoration of plasma osmolarity takes place But in SIADH ,secretion of ADH from tumor is not inhibited by hypotonic plasma
Signs and Symptoms Loss of appetite Weight loss Nausea and vomiting Headache Muscle weakness , spasm and cramps Fatigue Restlessness and irritability In severe conditions patient die because of coma and convulsions
Disorders of Pituitary Gland
Diabetes Insipidus Posterior Pituitary disorder characterized by excess excretion of water through urine

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Disorders of pituitary gland

  • 1. Pituitary gland Saddam Ansari Tbilisi State Medical University
  • 3. Causes of Disorder of Pituitary Gland Mainly of 2 reasons: Hyperactivity Hypoactivity
  • 6. Gigantism Pituitary disorder characterized by: Excess growth of body Average height is approximately 7 – 8 feet
  • 7. Continued… Causes of Gigantism Hypersecretion of GH in childhood or in pre – adult Tumor of acidophilic cells of Anterior pituitary
  • 8.
  • 9. Continued… Signs and Symptoms Huge stature : 7 or 8 feet height Hyperglycemia , develop glycosuria , pituitary diabetes mellitus Headache due to tumor of pituitary
  • 10. Continued… Visual disturbances Gigantism ends in hypopituitarism (burning of cells of anterior pituitary )
  • 11.
  • 13. Acromegaly Anterior pituitary disorder characterized by: Enlargement, thickening, and broadening of bones Particularly extremities of the body
  • 14. Continued… Causes of Acromegaly Hypersecretion of GH after fusion of epiphysis with shaft of bone Adenomatous tumor of anterior pituitary involving the acidophilic cells.
  • 15.
  • 16.
  • 17. Continued… Signs and symptoms Kyphosis : enlargement of hands and feet with bowing spine Scalp is thickened and thrown into folds Overgrowth of body hair Visceral organs are enlarged
  • 18.
  • 19. Continued… Signs and symptoms Thyroid , parathyroid and adrenal glands shows hyperactivity Hyperglycemia and glucosuria Hypertension Headache Visual disturbance – Bitemporal hemianopia
  • 20.
  • 21.
  • 23.
  • 24. Due to hypersecretion of GH in children,before fusion of epiphysis with the shaft of bone results in Gigantism
  • 25.
  • 27. Cushing’s Disease Rare disease characterized by obesity
  • 28. Continued… Cause Hypersecretion of glucocorticoids mainly cortisol Either pituitary origin or adrenal origin Cushing’s Cushing’s disease syndrome
  • 29. Continued… Pituitary origin Increased secretion of ACTH leads to hyperplasia of adrenal cortex therefore, hypersecretion of glucocorticoids takes place ACTH is increased by Tumor in pituitary cells ( basophilic cells) Malignant tumor of nonendocrine origin like cancer of lungs or abdominal viscera Hypothalamic disorder causing hypersecretion of corticotropin releasing hormone
  • 30. Continued… Signs and symptoms 1. Disproportionate distribution of body fat results: Moon face : Fat accumulation and retention of water and salt Torso : Fat accumulation in chest and abdomen but slim legs and arms Buffalo hump : Fat deposit on the back of neck and shoulder Pot belly : Fat accumulation in upper abdomen
  • 31.
  • 32.
  • 33. Rupture of subdermal tissues due to stretching
  • 34.
  • 35. Continued… 3. Thinning of extremities 4. Thinning of skin and subcutaneous tissues 5. Darkening of skin on neck (aconthosis) 6. Pigmentation of skin 7. Facial redness (facial plethora) 8. Weakening of muscle
  • 36. Continued… 9. Facial hair growth ( Hirsutism ) 10. Bone resorption leads to osteoporosis 11. Hyperglycemia due to gluconeogeneis leads adrenal diabetes and glycosuria 12. Hypertension 13. Immunosuppression resulting in susceptibility for infection 14. Poor healing
  • 38. Dwarfism Pituitary disorder in children characterized by stunted growth
  • 39.
  • 41. Atrophy of acidophilic cells in the adenohypophysis
  • 42. Tumor of chromophobes : nonfunctioning tumor , compresses and destroys the normal cells
  • 43.
  • 44. Types of Dwarfism Laron dwarfism Psychogenic dwarfism Dwarfism in dystrophiaadiposogenitalis
  • 45. Laron Dwarfism Genetical disorder Called as GH insensitivity Occurs due to presence of abnormal GH secretagogue receptors in liver GHS becomes abnormal due to mutation in genes responsible for receptor Doesn’t depend on amount of GH secretion , hormone can’t stimulate the growth due to abnormal GHS
  • 46. Psychogenic Dwarfism Due to extreme emotional deprivation or stress Deficiency of GH Also called as psychosocial dwarfism or Stress dwarfism
  • 47.
  • 49. Retarded development of genital organs
  • 50.
  • 51. Acromicria Rare disease in adults characterized by the atrophy of the extremities of the body
  • 52.
  • 53. Atrophy of acidophilic cells in the anterior pituitary
  • 55.
  • 56. Signs and Symptoms Atrophy and thinning of extremities ( major symptoms ) Associated with hypothyroidism Hyposecretion of adrenocortical hormone Person becomes lethargic and obese Loss of sexual function
  • 58. Simmond’s Disease Rare pituitary disease Also called as cachexia Occurs mostly in panhypopituitarism
  • 59. Signs and Symptoms Developing senile decay Senile decay is due to deficiency of hormone from target glands of anterior pituitary e.g. thyroid gland, adrenal cortex and the gonads Loss of hair and loss of teeth The skin on face becomes dry and wrinkled. ( most common )
  • 61.
  • 63. Syndrome of Inappropriate Hypersecretion of Antidiuretic hormone Disease characterized by loss of sodium through urine due to hypersecretion of ADH
  • 64. Causes Due to cerebral tumors, lung tumors and lung cancers because the tumor cells secrete ADH Normal secretion of ADH makes the plasma hypotonic Hypotonic solution inhibits the ADH secretion and restoration of plasma osmolarity takes place But in SIADH ,secretion of ADH from tumor is not inhibited by hypotonic plasma
  • 65. Signs and Symptoms Loss of appetite Weight loss Nausea and vomiting Headache Muscle weakness , spasm and cramps Fatigue Restlessness and irritability In severe conditions patient die because of coma and convulsions
  • 67. Diabetes Insipidus Posterior Pituitary disorder characterized by excess excretion of water through urine
  • 68. Causes Develops due to the deficiency of ADH which occurs in the following conditions: Lesion (injury) or degradation of supraoptic and paraventricular nuclei of hypothalamus Lesion in hypothalamo-hypophyseal tract Atrophy of posterior pituitary Inability of renal tubules to give response to ADH hormone. Called as Nephrogenic diabetic insipidus.
  • 69. Signs and Symptoms 1.Polyuria Excretion of large quantity of dilute urine with increased frequency of voiding is called polyuria Daily output is 4 to 12 liters. Due to absence of ADH ,the epithelial cells of distal convoluted tubule in the nephron and the collecting duct of the kidney becomes impermeable to water
  • 70. Continued… 2.Polydipsia Intake of excess water Because of polyuria ,thirst center in hypothalamus results in intake of large quantity of water
  • 71. Continued… 3.Dehydration In some cases ,the thirst center in the hypothalamus is also affected by the lesion Therefore water intake decreases in these patients and, the loss of water through urine is not compensated
  • 73. DystrophiaAdiposogenitalis Characterized by obesity and hypogonadism affecting mainly adolescent boys Also known as Frohlich syndrome or hypothalamic eunuchism
  • 74. Causes Hypoactivity of both anterior and posterior pituitary Tumor in pituitary gland and hypothalamic regions concerned with food intake and gonadal development Injury or atrophy of pituitary gland Genetic inablility of hypothalamus to secrete luteinizing hormone
  • 75. Symptoms Obesity (common feature) Sexual infantilism (failure to develop secondary sexual characters) Dwarfism occurs if disease starts in growing age Called as infantile or prepubertal type of Frohlich syndrome (in children) and adult type of Frohlich’s syndrome (in adults) Other features are loss of vision and diabetes